EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

benzyladenine
adenine, N6-benzyl-

Supplier Sponsors

Name:N-benzyl-7H-purin-6-amine
CAS Number: 1214-39-7Picture of molecule3D/inchi
Other(deleted CASRN):124786-41-0
ECHA EINECS - REACH Pre-Reg:214-927-5
FDA UNII: KXG6A989PS
Nikkaji Web:J1.764G
Beilstein Number:616790
MDL:MFCD00005572
XlogP3:2.10 (est)
Molecular Weight:225.25467000
Formula:C12 H11 N5
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:cosmetic ingredient for hair conditioning
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:colorless fine needles (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 233.00 °C. @ 760.00 mm Hg
Vapor Pressure:2.373000 mmHg @ 20.00 °C. (est)
Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w): 1.570
Soluble in:
 water, 60 mg/L @ 20 °C (exp)
 water, 1472 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: hair conditioning
 
Suppliers:
BOC Sciences
For experimental / research use only.
6-Benzylaminopurine 95%
Odor: characteristic
Use: 6-Benzylaminopurine, a purine-based first-generation synthetic cytokinin, could stimulate plant growth. 6-Benzylaminopurine is a purine-based first-generation synthetic cytokinin that could stimulate plant growth.
EMD Millipore
For experimental / research use only.
6-Benzylaminopurine
Glentham Life Sciences
6-Benzylaminopurine
Santa Cruz Biotechnology
For experimental / research use only.
6-Benzylaminopurine ≥99%
Sigma-Aldrich: Aldrich
For experimental / research use only.
6-Benzylaminopurine ReagentPlus®, ≥99.0% (HPLC)
sds
TCI AMERICA
For experimental / research use only.
N6-Benzyladenine >99.0%(HPLC)(T)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-mouse LD50 1300 mg/kg
SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.

oral-rat LD50 2125 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.

Dermal Toxicity:
skin-mouse LD50 > 5000 mg/kg
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.

subcutaneous-mouse LD50 > 2300 mg/kg
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 19, Pg. 336, 1972.

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
cosmetic ingredient for hair conditioning
Recommendation for benzyladenine usage levels up to:
 not for fragrance use.
 
Recommendation for benzyladenine flavor usage levels up to:
 not for flavor use.
 
Safety References:
European Food Safety Authority (EFSA) reference(s):

Retrospective analysis of the immunotoxic effects of plant protection products as reported in the Draft Assessment Reports for their peer review at EU level
View page or View pdf

Review of the existing maximum residue levels for 6-benzyladenine according to Article 12 of Regulation (EC) No 396/2005
View page or View pdf

EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):1214-39-7
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :62389
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
N-benzyl-7H-purin-6-amine
Chemidplus:0001214397
RTECS:AU6252200 for cas# 1214-39-7
 
References:
 N-benzyl-7H-purin-6-amine
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:1214-39-7
Pubchem (cid):62389
Pubchem (sid):135020588
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
KEGG (GenomeNet):C11263
HMDB (The Human Metabolome Database):HMDB39238
FooDB:FDB018775
Export Tariff Code:2933.90.8300
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
•accel plant growth regulator solution: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 0.18% gibberellin a4 mixt. with gibberellin a7 •agtrol 6-b: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 0.18% gibberellin a4 mixt. with gibberellin a7 •6-benzyladenine technical (2 products): active ingredient 99.0 and 97.90% n-(phenylmethyl)-1h-purin-6-amine •ba6 technical: active ingredient 98.2% n-(phenylmethyl)-1h-purin-6-amine •bap-technical: active ingredient 98.80% n-(phenylmethyl)-1h-purin-6-amine •chrysal bvb: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 1.80% gibberellin a4 mixt. with gibberellin a7 •configure and exilis plus: active ingredient 2.00% n-(phenylmethyl)-1h-purin-6-amine •lt biosyn 6-benzylaminopurine technical: active ingredient 99.0% n-(phenylmethyl)-1h-purin-6-amine •maxcel: active ingredient 1.90% n-(phenylmethyl)-1h-purin-6-amine •perlan: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 1.80% gibberellin a4 mixt. with gibberellin a7 •promalin plant growth regulator solution: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 1.80% gibberellin a4 mixt. with gibberellin a7 •riteway: active ingredient 1.90% n-(phenylmethyl)-1h-purin-6-amine •typy plant growth regulator: active ingredients 1.80% n-(phenylmethyl)-1h-purin-6-amine and 1.80% gibberellin a4 mixt. with gibberellin a7 •paste •6-benzylaminopurine technical •water soluble concentrate
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 celery seed
Search Trop Picture
 not found in nature
 tomato
Search Trop Picture
 
Synonyms:
 adenine, N-benzyl-
 adenine, N(sup 6)-benzyl-
 adenine, N6-benzyl-
 aminopurine, 6-benzyl
 benzyl adenine
6-benzyl adenine
6-benzyl aminopurine
N-benzyl-1H-purin-6-amine
N-benzyl-3H-purin-6-amine
N-benzyl-7H-purin-6-amine
N-benzyl-9H-purin-6-amine
N6-benzyl-9H-purin-6-amine
N-benzyl-9H-purin-6-amine, N-(9H-Purin-6-yl)benzylamine
 benzyl(purin-6-yl)amine
6-(N-benzyl)aminopurine
6-benzyladenine
N-6-benzyladenine
N(Sup6)-benzyladenine
N6-benzyladenine
N-benzyladenine, 8CI
6-(benzylamino)-9H-purine
6-(benzylamino)purine
6-(N-benzylamino)purine
 benzylaminopurine
6-benzylaminopurine
 benzylpurin-6-ylamine
 paturyl
N-(phenylmethyl)-1H-purin-6-amine
N-(phenylmethyl)-1H-purine-6-amine
N-(phenylmethyl)-9H-purin-6-amine
6-[(phenylmethyl)amino]-9H-purine
 promalin
1H-purin-6-amine, N-(phenylmethyl)-
7H-purin-6-amine, N-(phenylmethyl)-
9H-purin-6-amine, N-(phenylmethyl)-
N-(9H-purin-6-yl)benzylamine
9H-purine, 6-[(phenylmethyl)amino]-
 

Articles:

PubMed:Rapid in vitro propagation system through shoot tip cultures of Vitex trifolia L.-an important multipurpose plant of the Pacific traditional Medicine.
PubMed:Efficient regeneration for enhanced steviol glycosides production in Stevia rebaudiana (Bertoni).
PubMed:Dissipation kinetics of forchlorfenuron, 6-benzyl aminopurine, gibberellic acid and ethephon residues in table grapes (Vitis vinifera).
PubMed:Early induction of apple fruitlet abscission is characterized by an increase of both isoprene emission and abscisic acid content.
PubMed:6-Benzylaminopurine alleviates chilling injury of postharvest cucumber fruit through modulating antioxidant system and energy status.
PubMed:Opening of Iris flowers is regulated by endogenous auxins.
PubMed:Protocol for augmented shoot organogenesis in selected variety of soybean [Glycine max L. (Merr.)].
PubMed:Maintaining quality and bioactive compounds of broccoli by combined treatment with 1-methylcyclopropene and 6-benzylaminopurine.
PubMed:Effects of different combinations of benzyl adenine and indole acetic acid concentrations on in vitro plant regeneration in hexaploid wheat.
PubMed:Enhancement of folate content and its stability using food grade elicitors in coriander (Coriandrum sativum L.).
PubMed:A protocol for transformation of Torenia.
PubMed:6-Benzylaminopurine delays senescence and enhances health-promoting compounds of harvested broccoli.
PubMed:Leaf volatiles and secretory cells of Alpinia zerumbet (Pers.) Burtt et Smith (Zingiberaceae).
PubMed:Enhancing antioxidant availability in wheat grains from plants grown under seawater stress in response to microalgae extract treatments.
PubMed:6-benzyladenine metabolism during reinvigoration of mature Pinus radiata buds in vitro.
PubMed:Influence of growth regulators in biomass production and volatile profile of in vitro plantlets of Thymus vulgaris L.
PubMed:Micropropagation of ornamental Prunus spp. and GF305 peach, a Prunus viral indicator.
PubMed:In vitro clonal propagation of bird eye chilli (Capsicum frutescens Mill.).
PubMed:Efficient clonal propagation method for Decalepis hamiltonii, an endangered shrub, under the influence of phloroglucinol.
PubMed:Somatic embryogenesis from leaf explants of Australian fan flower, Scaevola aemula R. Br.
PubMed:In vitro antibacterial, antifungal, and antioxidant activities of the essential oil and methanol extracts of herbal parts and callus cultures of Satureja hortensis L.
PubMed:Increasing resistance against Phytophthora citrophthora in tangelo Nova fruits by modulating polymethoxyflavones levels.
PubMed:Synthesis and cytokinin activity of fluorescent 7-Phenylethynylimidazo[4,5-b]pyridine and its riboside.
PubMed:Tissue culture based screening for selection of high biomass and phenolic producing clonal lines of lavender using pseudomonas and azetidine-2-carboxylate.
PubMed:Stimulation of benzyladenine-induced in vitro shoot organogenesis and endogenous proline in melon (Cucumis melo L.) by fish protein hydrolysates in combination with proline analogues.
PubMed:In vitro food production for isolated closed environments: formation of ripe tomato fruits from excised flower buds.
PubMed:Effects of benzyladenine on cotyledon metabolism and growth of peas.
 
Notes:
6-Benzylaminopurine, benzyl adenine or BAP is a first-generation synthetic cytokinin which elicits plant growth and development responses, setting blossoms and stimulating fruit richness by stimulating cell division. It is an inhibitor of respiratory kinase in plants, and increases post-harvest life of green vegetables. (Wikipedia)
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